Gene · 64072
Papers1,428
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
101 to 120 of 1,428
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| GelMA/PEDOT:PSS Composite Conductive Hydrogel-Based Generation and Protection of Cochlear Hair Cells through Multiple Signaling Pathways. | Biomolecules | 2024 | 38254695 | PubTator, text mining | PubMed |
| Interactions of genetic variations in FAS, GJB2 and PTPRN2 are associated with noise-induced hearing loss: a case-control study in China. | BMC Med Genomics | 2024 | 38212800 | PubTator, text mining | PubMed |
| Outcomes and effect of somatic mutations after erythropoiesis stimulating agents in patients with lower-risk myelodysplastic syndromes. | Ther Adv Hematol | 2024 | 38186638 | PubTator, text mining | PubMed |
| Novel compound heterozygous MYO15A splicing variants in autosomal recessive non-syndromic hearing loss. | BMC Med Genomics | 2024 | 38167320 | PubTator, text mining | PubMed |
| Genetic correction of induced pluripotent stem cells from a DFNA36 patient results in morphologic and functional recovery of derived hair cell-like cells. | Stem Cell Res Ther | 2024 | 38167128 | PubTator, text mining | PubMed |
| Using the Bayesian variational spike and slab model in a genome-wide association study for finding associated loci with bipolar disorder. | Ann Hum Genet | 2024 | 38161273 | PubTator, text mining | PubMed |
| The RRAS2 pathogenic variant (c.67G>T; p. Gly23Cys) produces Noonan syndrome with embryonal rhabdomyosarcoma. | Mol Genet Genomic Med | 2024 | 37942564 | PubTator, text mining | PubMed |
| Whole-genome resequencing reveals new mutations in candidate genes for Beichuan-white goat prolificacya. | Anim Biotechnol | 2024 | 37729465 | PubTator, text mining | PubMed |
| Integrated analysis of single-cell and bulk RNA sequencing data reveals immune-related lncRNA-mRNA prognostic signature in triple-negative breast cancer. | Genes Dis | 2024 | 37692501 | PubTator, text mining | PubMed |
| Pediatric Macrocorticotropinoma: Do They Differ from Microcorticotropinoma? | Neuroendocrinology | 2024 | 37634509 | PubTator, text mining | PubMed |
| An aggressive cabergoline-resistant, temozolomide-responsive macroprolactinoma due to a germline SDHB pathogenic variant in the absence of paraganglioma or pheochromocytoma. | Front Endocrinol (Lausanne) | 2023 | 38152133 | PubTator, text mining | PubMed |
| Identification of a novel compound heterozygous pathogenic variant in MYO7A causing Usher syndrome type IB in a Chinese patient: a case report. | J Int Med Res | 2023 | 38141656 | PubTator, text mining | PubMed |
| Random Allelic Expression in Inherited Retinal Disease Genes. | Curr Issues Mol Biol | 2023 | 38132471 | PubTator, text mining | PubMed |
| Treatment following Triple-AAV Delivery in Mature Murine Model of Human CDH23-Associated Hearing Loss. | Curr Issues Mol Biol | 2023 | 38132436 | PubTator, text mining | PubMed |
| Which Came First? When Usher Syndrome Type 1 Couples with Neuropsychiatric Disorders. | Audiol Res | 2023 | 38131811 | PubTator, text mining | PubMed |
| Quantitative thresholds for variant enrichment in 13,845 cases: improving pathogenicity classification in genetic hearing loss. | Genome Med | 2023 | 38111038 | PubTator, text mining | PubMed |
| Traditional Chinese medicine for the prevention and treatment of presbycusis. | Heliyon | 2023 | 38076135 | PubTator, text mining | PubMed |
| The Relevance of Autophagy within Inner Ear in Baseline Conditions and Tinnitus-Related Syndromes. | Int J Mol Sci | 2023 | 38068993 | PubTator, text mining | PubMed |
| Accurate phenotypic classification and exome sequencing allow identification of novel genes and variants associated with adult-onset hearing loss. | PLoS Genet | 2023 | 38011198 | PubTator, text mining | PubMed |
| Prognostic potential of whole exome sequencing in the clinical management of metachronous colorectal cancer liver metastases. | Cancer Cell Int | 2023 | 38008721 | PubTator, text mining | PubMed |
gene-search-2026-11-11-0.2.0
Sources 12
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ChEMBL, through Open TargetsCC BY-SA 3.0
- ClinicalTrials.govNo license stated
- EMBL-EBI's patent proteinsNo added restrictions. Attribution expected
- GenBank's patent filesNo restrictions from NCBI. Submitters may hold rights
- HGNCCC0
- NCBI GenePublic domain (US government)
- NIH's project files and grant-paper linksPublic domain
- Open TargetsCC0 1.0
- PubMedNLM's terms
- PubTator 3Public domain
- UniProtCC BY 4.0
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
- ClinicalTrials.govnone stated
- EMBL-EBI's patent proteinsEMBL-EBI's patent protein files from the EPO, JPO, KIPO and USPTO. EMBL-EBI: "EMBL-EBI itself places no additional restrictions on the use or redistribution of the data available via its Data Resources and Tools other than those provided by the original data owners" and "EMBL-EBI expects attribution (e.g. in publications, services or products) for the use of any of its Data Resources and Tools." Read on 11 Nov 2026 at https://www.ebi.ac.uk/about/terms-of-use
- GenBank's patent filesGenBank's patent files. NCBI: "NCBI places no restrictions on the use or distribution of the GenBank data. However, some submitters may claim patent, copyright, or other intellectual property rights in all or a portion of the data they have submitted." Read on 11 Nov 2026 at https://www.ncbi.nlm.nih.gov/genbank/about/
- HGNCCC0: https://www.genenames.org/about/license/
- NCBI GeneNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
- NIH's project files and grant-paper linksPublic domain (NIH RePORTER)
- Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
- PubMedNLM's terms
- PubTator 3Public domain
- UniProtCC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
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GET https://conductscience.org/api/genes/v1/64072/papers?page=6